Aim of the study is to compare safety and tolerance of two techniques of Video Assisted Thoracic Surgery (VATS) uniportal lobectomies in the prospective randomized single-institutional trial. One arm is a uniportal lobectomy performed through the transcervical approach with elevation of the sternum, the other arm will utilize a standard uniportal intercostal approache. There will be 10 patients in each group. Patients in clinical stage cI-III (T1-3N0-2M0) Non-Small Cell Lung Cancer (NSCLC). The results will be compared for time of the procedure, number of conversions to multi-portal VATS and/or open thoracotomy, duration and volume of chest drainage, amount of postoperatve pain, time of hospitalization and the number of resected lymph nodes and metastatic nodes. Accrual of patients is planned to complete within 12 months.
Age range
18 Years – 85 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
time of the procedure
Timeframe: 4 weeks
number of conversions to multi-portal VATS and/or open thoracotomy
Timeframe: 4 weeks
duration of chest drainage
Timeframe: 4 weeks
volume of chest drainage
Timeframe: 4 weeks
amount of postoperatve pain
Timeframe: up to 72 hours after the end of surgery
time of hospitalization
Timeframe: 4 weeks
number of resected lymph nodes
Timeframe: 4 weeks
number of resected metastatic nodes
Timeframe: 4 weeks